Mipomersen, an apolipoprotein B synthesis inhibitor, for lowering of LDL cholesterol concentrations in patients with homozygous familial hypercholesterolaemia: a randomised, double-blind, placebo-controlled trial.

Author: BlomDirk J, CharngMin-Ji, Chasan-TaberScott, CromwellWilliam C, CrookeStanley T, FlaimJoann D, GaudetDaniel, LachmannRobin H, MaraisA David, RaalFrederick J, SantosRaul D, TanJu L, TribbleDiane L

Paper Details 
Original Abstract of the Article :
Homozygous familial hypercholesterolaemia is a rare genetic disorder in which both LDL-receptor alleles are defective, resulting in very high concentrations of LDL cholesterol in plasma and premature coronary artery disease. This study investigated whether an antisense inhibitor of apolipoprotein B ...See full text at original site
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引用元:
https://doi.org/10.1016/S0140-6736(10)60284-X

データ提供:米国国立医学図書館(NLM)

Mipomersen: A New Hope for Homozygous Familial Hypercholesterolaemia

The realm of [lipid metabolism] presents unique challenges when addressing [homozygous familial hypercholesterolaemia], a rare genetic disorder characterized by extremely high levels of [LDL cholesterol]. This study investigates the efficacy and safety of [mipomersen], an [antisense inhibitor of apolipoprotein B synthesis], as an adjunctive therapy to lower [LDL cholesterol] in patients with this debilitating condition. The authors demonstrate the potential of [mipomersen] to significantly reduce [LDL cholesterol] levels, offering a glimmer of hope for patients facing the devastating consequences of this disease.

A Ray of Light in the Desert of Hypercholesterolaemia

The authors shed light on the potential of [mipomersen] to offer significant benefits for patients with [homozygous familial hypercholesterolaemia]. This research provides a glimmer of hope in the desert of this rare and challenging condition, offering a promising new treatment option for those affected by this debilitating disease.

Navigating the Desert of Lipid Management: A New Tool for Clinicians

This research equips clinicians with a valuable new tool to combat the challenges of [homozygous familial hypercholesterolaemia]. The authors provide evidence-based information to guide treatment decisions, demonstrating the efficacy and safety of [mipomersen] in lowering [LDL cholesterol] levels. This research provides an oasis of knowledge in the vast desert of lipid management.

Dr.Camel's Conclusion

This study is a reminder that even in the most desolate areas of medical knowledge, we can find hope and innovation. The development of [mipomersen] represents a significant step forward in the treatment of [homozygous familial hypercholesterolaemia], offering a glimmer of hope for patients facing a challenging journey. Let us embrace this research as a reminder to never cease exploring the vast desert of medical knowledge, seeking new solutions to improve patient outcomes.

Date :
  1. Date Completed 2010-05-03
  2. Date Revised 2015-06-16
Further Info :

Pubmed ID

20227758

DOI: Digital Object Identifier

10.1016/S0140-6736(10)60284-X

Related Literature

SNS
PICO Info
in preparation
Languages

English

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